Please choose an event type to view the corresponding MedsFacts report:

RENAL FAILURE ACUTE ( 160 FDA reports)
RETINAL VEIN THROMBOSIS ( 160 FDA reports)
MEDICAL DEVICE COMPLICATION ( 14 FDA reports)
DEVICE BREAKAGE ( 14 FDA reports)
DIABETIC FOOT INFECTION ( 12 FDA reports)
SKIN ULCER ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
FATIGUE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
JAUNDICE ( 7 FDA reports)
DIARRHOEA ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
COMA ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
MUCOSAL INFECTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
DEHYDRATION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
COLITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
HEADACHE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
DEATH ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)

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